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10 Facts About the Food and Drug Administration

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The Food and Drug Administration is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments.

The United States federal executive departments are among the oldest primary units of the executive branch of the federal government of the United States—the Departments of State, War, and the Treasury all having been established within a few weeks of each other in 1789.

The United States Department of Health and Human Services, also known as the Health Department, is a cabinet-level department of the U.S. federal government with the goal of protecting the health of all Americans and providing essential human services.

The United States of America, commonly referred to as the United States or America, is a federal republic composed of ‹See TfD›50 states, a federal district, five major self-governing territories, and various possessions.

How Does The FDA Approve New Drugs? by Seeker Daily

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The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices, cosmetics, animal foods & feed and veterinary products.

A medical device is any instrument, apparatus, appliance, software, material, or other article—whether used alone or in combination, including the software intended by its manufacturer to be used specifically for diagnostic and/or therapeutic purposes and necessary for its proper application—intended by the manufacturer to be used for human beings for the purpose of:

Public health refers to "the science and art of preventing disease, prolonging life and promoting health through organized efforts and informed choices of society, organizations, public and private, communities and individuals."

A biopharmaceutical, also known as a biologic medical product, biological, or biologic, is any pharmaceutical drug product manufactured in, extracted from, or semisynthesized from biological sources.

Mga kending nakalason umano, hawak na ng FDA by ABS-CBN News

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The FDA was empowered by the United States Congress to enforce the Federal Food, Drug, and Cosmetic Act, which serves as the primary focus for the Agency; the FDA also enforces other laws, notably Section 361 of the Public Health Service Act and associated regulations, many of which are not directly related to food or drugs.

The United States Federal Food, Drug, and Cosmetic Act, is a set of laws passed by Congress in 1938 giving authority to the U.S. Food and Drug Administration to oversee the safety of food, drugs, and cosmetics.

The United States Congress is the bicameral legislature of the federal government of the United States consisting of two chambers: the Senate and the House of Representatives.

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These include regulating lasers, cellular phones, condoms and control of disease on products ranging from certain household pets to sperm donation for assisted reproduction.

A pet or companion animal is an animal kept primarily for a person's company or protection, as opposed to working animals, sport animals, livestock, and laboratory animals, which are kept primarily for performance, agricultural value, or research.

Assisted reproductive technology is the technology used to achieve pregnancy in procedures such as fertility medication, in vitro fertilization and surrogacy.

A mobile phone is a portable telephone that can make and receive calls over a radio frequency link while the user is moving within a telephone service area.

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The FDA is led by the Commissioner of Food and Drugs, appointed by the President with the advice and consent of the Senate.

Advice and consent is an English phrase frequently used in enacting formulae of bills and in other legal or constitutional contexts.

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The Commissioner reports to the Secretary of Health and Human Services.

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Dr. Robert M. Califf, MD is the current commissioner, who took over in February 2016 for Dr. Stephen Ostroff, who had been acting since April 2015.

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The FDA has its headquarters in unincorporated White Oak, Maryland.

Maryland is a state located in the Mid-Atlantic region of the United States, bordering Virginia, West Virginia, and Washington, D.C. to its south and west; Pennsylvania to its north; and Delaware to its east.

Headquarters denotes the location where most, if not all, of the important functions of an organization are coordinated.

White Oak is a census-designated place and an unincorporated area in Montgomery County, Maryland, United States.

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The agency also has 223 field offices and 13 laboratories located throughout the 50 states, the United States Virgin Islands, and Puerto Rico.

Puerto Rico, officially the Commonwealth of Puerto Rico and formerly known as and sometimes called Porto Rico, is the largest insular territory of the United States, and it is located in the northeastern Caribbean Sea.

The United States Virgin Islands, officially the Virgin Islands of the United States, are a group of islands in the Caribbean that are an insular area of the United States.

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In 2008, the FDA began to post employees to foreign countries, including China, India, Costa Rica, Chile, Belgium, and the United Kingdom.

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